Wide nose

Symptom Information:

Symptom ID: HPO:0000445
Synonyms:
Broad nose [HPO:0000445]
Wide nose (finding) [Orphanet:8090]
Wide nose [Orphanet:8090]
Broad nose [OMIM:Broad nose]
Wide nose [OMIM:Wide nose]
Broad nose/nasal bridge [Orphanet:8090]
Quality:
Cross references:
Orphanet:8090 "Broad nose/nasal bridge" [Orphanet:8090]
OMIM: "Broad nose" [OMIM:Broad nose]
OMIM: "Wide nose" [OMIM:Wide nose]
UMLS:C0426421 "Wide nose" [Orphanet:8090]
Is a (Direct Parents):
Orphanet Wide nasal bridge
Orphanet Abnormality of the nose
HPO         Abnormal nasal morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Abnormal nasal morphology(HPO:0005105)
                      Wide nose(HPO:0000445)
MedDRA:
Database Frequency: 190 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
14q11.2 microdeletion syndrome (Orphanet:261120)
15q24 microdeletion syndrome (Orphanet:94065)
16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
16p13.11 microdeletion syndrome (Orphanet:261236)
17p13.3 microduplication syndrome (Orphanet:217385)
1q21.1 microdeletion syndrome (Orphanet:250989)
20p12.3 microdeletion syndrome (Orphanet:261295)
22q11.2 microduplication syndrome (Orphanet:1727)
3q13 microdeletion syndrome (Orphanet:1621)
49,XXXXY syndrome (Orphanet:96264)
8p23.1 microdeletion syndrome (Orphanet:251071)
8p23.1 microduplication syndrome (Orphanet:251076)
8q21.11 microdeletion syndrome (Orphanet:284160)
8q22.1 microdeletion syndrome (Orphanet:178303)
ADULT syndrome (Orphanet:978)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrodysostosis (Orphanet:950)
Acromegaly (Orphanet:963)
Acromelic frontonasal dysplasia (Orphanet:1827)
Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Ascher syndrome (Orphanet:1253)
Aspartylglucosaminuria (Orphanet:93)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Auriculoocular anomalies - cleft lip (Orphanet:71270)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive chorioretinopathy-microcephaly (Orphanet:2518)
Autosomal recessive cutis laxa type 2 (Orphanet:90350)
Axenfeld-Rieger syndrome (Orphanet:782)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Baraitser-Winter syndrome (Orphanet:2995)
Barber-Say syndrome (Orphanet:1231)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Bohring-Opitz syndrome (Orphanet:97297)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Branchio-oculo-facial syndrome (Orphanet:1297)
CHARGE syndrome (Orphanet:138)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
Camptodactyly - fibrous tissue hyperplasia - skeletal dysplasia (Orphanet:1321)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cartilage-hair hypoplasia (Orphanet:175)
Central diabetes insipidus (Orphanet:178029)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Charlie M syndrome (Orphanet:1406)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Cloverleaf skull - multiple congenital anomalies (Orphanet:93267)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Cold-induced sweating syndrome (Orphanet:157820)
Craniodiaphyseal dysplasia (Orphanet:1513)
Craniofacial dyssynostosis (Orphanet:1516)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniorhiny (Orphanet:157832)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Deafness - onychodystrophy (Orphanet:3231)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal monosomy 10p (Orphanet:1580)
Distal monosomy 6p (Orphanet:96125)
Dysmorphism - short stature - deafness - disorder of sex development (Orphanet:2282)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Epiphyseal dysplasia - hearing loss - dysmorphism (Orphanet:1825)
Ermine phenotype (Orphanet:999)
FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES,AND SPONTANEOUS FILTERING BLEBS (OMIM:601552)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Facial dysmorphism - shawl scrotum - joint laxity (Orphanet:1778)
Facial ectodermal dysplasia (Orphanet:1807)
Filippi syndrome (Orphanet:3255)
Fraser syndrome (Orphanet:2052)
Freeman-Sheldon syndrome (Orphanet:2053)
Frontonasal dysplasia (Orphanet:250)
Fryns syndrome (Orphanet:2059)
Fucosidosis (Orphanet:349)
GCS1-CDG (Orphanet:79330)
GM1 gangliosidosis (Orphanet:354)
Geleophysic dysplasia (Orphanet:2623)
Genitopatellar syndrome (Orphanet:85201)
German syndrome (Orphanet:2077)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Hennekam syndrome (Orphanet:2136)
Hennekam-Beemer syndrome (Orphanet:2135)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hydrocephaly - low insertion umbilicus (Orphanet:2184)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypertelorism, Teebi type (Orphanet:1519)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus (Orphanet:3044)
Intellectual deficit - short stature - hypertelorism (Orphanet:3074)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy (Orphanet:2958)
Intellectual deficit, X-linked, Siderius type (Orphanet:85287)
Isotretinoin-like syndrome (Orphanet:2306)
Jacobsen syndrome (Orphanet:2308)
Juberg-Hayward syndrome (Orphanet:2319)
Jung-Wolff-Back-Stahl syndrome (Orphanet:2321)
Keipert syndrome (Orphanet:2662)
Keutel syndrome (Orphanet:85202)
Langer-Giedion syndrome (Orphanet:502)
Laurin-Sandrow syndrome (Orphanet:2378)
Lethal multiple pterygium syndrome (Orphanet:33108)
Lethal recessive chondrodysplasia (Orphanet:1423)
Léri-Weill dyschondrosteosis (Orphanet:240)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35 (OMIM:615162)
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM (OMIM:616033)
MULTIPLE SYNOSTOSES SYNDROME 2 (OMIM:610017)
Marshall syndrome (Orphanet:560)
Megalencephaly (Orphanet:2477)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Microcephalic primordial dwarfism, Alazami type (Orphanet:319671)
Microcephaly - brachydactyly - kyphoscoliosis (Orphanet:3433)
Microcephaly - intellectual deficit - phalangeal and neurological anomalies (Orphanet:137658)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Microcephaly - seizures - intellectual deficit - heart disease (Orphanet:2519)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Microcornea-myopic chorioretinal atrophy-telecanthus syndrome (Orphanet:369970)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mietens syndrome (Orphanet:2557)
Monosomy 13q14 (Orphanet:1587)
Monosomy 18p (Orphanet:1598)
Mosaic trisomy 14 (Orphanet:1703)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mowat-Wilson syndrome (Orphanet:2152)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Muckle-Wells syndrome (Orphanet:575)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Neonatal adrenoleukodystrophy (Orphanet:44)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
Noonan syndrome with multiple lentigines (Orphanet:500)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Opitz G/BBB syndrome (Orphanet:2745)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteocraniostenosis (Orphanet:2763)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Patent arterial duct (Orphanet:706)
Paternal 20q13.2q13.3 microdeletion syndrome (Orphanet:261304)
Pentasomy X (Orphanet:11)
Pierre Robin syndrome - faciodigital anomaly (Orphanet:2888)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Rabson-Mendenhall syndrome (Orphanet:769)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
Ring chromosome 10 (Orphanet:1438)
Say-Field-Coldwell syndrome (Orphanet:3133)
Scheie syndrome (Orphanet:93474)
Sclerosteosis (Orphanet:3152)
Short rib-polydactyly syndrome, Verma-Naumoff type (Orphanet:93271)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Spondyloepimetaphyseal dysplasia with multiple dislocations (Orphanet:93360)
Spondyloepimetaphyseal dysplasia, Geneviève type (Orphanet:168454)
Summitt syndrome (Orphanet:3210)
Symptomatic form of Coffin-Lowry syndrome in female carriers (Orphanet:276630)
Syndromic diarrhea (Orphanet:84064)
TEMPLE SYNDROME (OMIM:616222)
TEMPLE-BARAITSER SYNDROME (OMIM:611816)
TENORIO SYNDROME (OMIM:616260)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
Trisomy 17p (Orphanet:261290)
Trisomy 1q (Orphanet:261344)
Van den Ende-Gupta syndrome (Orphanet:2460)
W syndrome (Orphanet:2804)
Waardenburg-Shah syndrome (Orphanet:897)
Weaver-Williams syndrome (Orphanet:3448)
Wiedemann-Steiner syndrome (Orphanet:319182)
Williams syndrome (Orphanet:904)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked intellectual deficit, Najm type (Orphanet:163937)
Zechi-Ceide syndrome (Orphanet:217017)
Zellweger syndrome (Orphanet:912)
Zimmermann-Laband syndrome (Orphanet:3473)